Research Progress on Plant Anti-Freeze Proteins

Plant antifreeze proteins(AFPs)are special proteins that can protect plant cells from ice crystal damage in low-temperature environments,and they play a crucial role in the process of plants adapting to cold environ-ments.Proteins with these characteristics have been found infish living in cold regions,as well as many plants and insects.Although research on plant AFPs started relatively late,their application prospects are broad,leading to the attention of many researchers to the isolation,cloning,and genetic improvement of plant AFP genes.Studies have found that the distribution of AFPs in different species seems to be the result of independent evolu-tionary events.Unlike the AFPs found infish and insects,plant AFPs have multiple hydrophilic ice-binding domains,and their recrystallization inhibition activity is about 10–100 times that offish and insect AFPs.Although different plant AFPs have the characteristics of low TH and high RI,their DNA and amino acid sequences are completely different,with small homology.With in-depth research and analysis of the character-istics and mechanisms of plant AFPs,not only has our understanding of plant antifreeze mechanisms been enriched,but it can also be used to improve crop varieties and enhance their freezing tolerance,yield,and quality through genetic engineering.In addition,the study of plant AFPs also contributes to our understanding of freezing resistance mechanisms in other organisms and provides new research directions for thefield of biotech-nology.Therefore,based on the analysis of relevant literature,this article will delve into the concepts,character-istics,research methods,and mechanisms of plant AFPs,summarize the latest research progress and application prospects of AFPs in plant,and provide prospects for the future development of AFP gene research.

An intrinsically self-healing and anti-freezing molecular chains induced polyacrylamide-based hydrogel electrolytes for zinc manganese dioxide batteries

The anti-freezing strategy of hydrogels and their self-healing structure are often contradictory,it is vital to break through the molecular structure to design and construct hydrogels with intrinsic anti-freezing/self-healing for meeting the rapid development of flexible and wearable devices in diverse service conditions.Herein,we design a new hydrogel electrolyte(AF/SH-Hydrogel)with intrinsic anti-freezing/self-healing capabilities by introducing ethylene glycol molecules,dynamic chemical bonding(disulfide bond),and supramolecular interaction(multi-hydrogen bond)into the polyacrylamide molecular chain.Thanks to the exceptional freeze resistance(84%capacity retention at-20℃)and intrinsic self-healing capabilities(95%capacity retention after 5 cutting/self-healing cycles),the obtained AF/SH-Hydrogel makes the zinc||manganese dioxide cell an economically feasible battery for the state-of-the-art applications.The Zn||AF/SH-Hydrogel||MnO_(2)device offers a near-theoretical specific capacity of 285 m A h g^(-1)at 0.1 A g^(-1)(Coulombic efficiency≈100%),as well as good self-healing capability and mechanical flexibility in an ice bath.This work provides insight that can be utilized to develop multifunctional hydrogel electrolytes for application in next generation of self-healable and freeze-resistance smart aqueous energy storage devices.

An Investigation of Freezing of Supercooled Water on Anti-Freeze Protein Modified Surfaces

This work investigates how functionalization of aluminium surfaces with natural type III Anti-Freeze Protein （AFP） affects the mechanism of heterogeneous ice nucleation. First the bulk ice nucleation properties of distilled water and aqueous solution of AFP were evaluated by differential scanning calorimetry. Then the modified surface was characterized by Secondary Ions Mass Spectroscopy （SIMS）, Fourier Transform InfraRed （FTIR） spectroscopy and contact angle measurement. Freezing experiments were then conducted in which water droplets underwent a slow controlled cooling. This study shows that compared to uncoated aluminium, the anti-freeze proteins functionalized surfaces exhibit a higher and narrower range of freezing temperature. It was found that these proteins that keep living organisms from freezing in cold environment act in the opposite way once immobilized on surfaces by promoting ice nucleation. Some suggestions regarding the mechanism of action of the observed phenomena were proposed based on the Classical Nucleation Theory （CNT）.

Wide temperature range-and damage-tolerant microsupercapacitors from salt-tolerant, anti-freezing and self-healing organohydrogel via dynamic bonds modulation

The advance of microelectronics requires the micropower of microsupercapacitors(MSCs) to possess wide temperature-and damage-tolerance beyond high areal energy density.The properties of electrolyte are crucial for MSCs to meet the above requirements.Here,an organohydrogel electrolyte,featured with high salt tolerance,ultralow freezing point,and strong self-healing ability,is experimentally realized via modulating its inner dynamic bonds.Spectroscopic and theoretical analysis reveal that dimethyl sulfoxide has the ability to reconstruct Li^(+)solvation structure,and interact with free water and polyvinyl alcohol chains via forming hydrogen bonds.The organohydrogel electrolyte is employed to build MSCs,which show a boosted energy density,promising wide temperature range-and damage-tolerant ability.These attractive features make the designed organohydrogel electrolyte have great potential to advance MSCs.

Mechanical reliable,NIR light-induced rapid self-healing hydrogel electrolyte towards flexible zinc-ion hybrid supercapacitors with low-temperature adaptability and long service life

Hydrogel electrolytes hold great potential in flexible zinc ion supercapacitors(ZICs)due to their high conductivity,good safety,and flexibility.However,freezing of electrolytes at low temperature(subzero)leads to drastic reduction in ionic conductivity and mechanical properties that deteriorates the performance of flexible ZICs.Besides,the mechanical fracture during arbitrary deformations significantly prunes out the lifespan of the flexible device.Herein,a Zn^(2+)and Li^(+)co-doped,polypyrrole-dopamine decorated Sb_(2)S_(3)incorporated,and polyvinyl alcohol/poly(N-(2-hydroxyethyl)acrylamide)double-network hydrogel electrolyte is constructed with favorable mechanical reliability,anti-freezing,and self-healing ability.In addition,it delivers ultra-high ionic conductivity of 8.6 and 3.7 S m^(-1)at 20 and−30°C,respectively,and displays excellent mechanical properties to withstand tensile stress of 1.85 MPa with tensile elongation of 760%,together with fracture energy of 5.14 MJ m^(-3).Notably,the fractured hydrogel electrolyte can recover itself after only 90 s of infrared illumination,while regaining 83%of its tensile strain and almost 100%of its ionic conductivity during−30–60°C.Moreover,ZICs coupled with this hydrogel electrolyte not only show a wide voltage window(up to 2 V),but also provide high energy density of 230 Wh kg^(-1)at power density of 500 W kg^(-1)with a capacity retention of 86.7%after 20,000 cycles under 20°C.Furthermore,the ZICs are able to retain excellent capacity even under various mechanical deformation at−30°C.This contribution will open up new insights into design of advanced wearable flexible electronics with environmental adaptability and long-life span.

Coupling of Adhesion and Anti‑Freezing Properties in Hydrogel Electrolytes for Low‑Temperature Aqueous‑Based Hybrid Capacitors

Solid-state zinc-ion capacitors are emerging as promising candidates for large-scale energy storage owing to improved safety,mechanical and thermal stability and easy-to-direct stacking.Hydrogel electrolytes are appealing solid-state electrolytes because of eco-friendliness,high conductivity and intrinsic flexibility.However,the electrolyte/electrode interfacial contact and anti-freezing properties of current hydrogel electrolytes are still challenging for practical applications of zinc-ion capacitors.Here,we report a class of hydrogel electrolytes that couple high interfacial adhesion and anti-freezing performance.The synergy of tough hydrogel matrix and chemical anchorage enables a well-adhered interface between hydrogel electrolyte and electrode.Meanwhile,the cooperative solvation of ZnCl2 and LiCl hybrid salts renders the hydrogel electrolyte high ionic conductivity and mechanical elasticity simultaneously at low temperatures.More significantly,the Zn||carbon nanotubes hybrid capacitor based on this hydrogel electrolyte exhibits low-temperature capacitive performance,delivering high-energy density of 39 Wh kg^(-1)at-60°C with capacity retention of 98.7%over 10,000 cycles.With the benefits of the well-adhered electrolyte/electrode interface and the anti-freezing hydrogel electrolyte,the Zn/Li hybrid capacitor is able to accommodate dynamic deformations and function well under 1000 tension cycles even at-60°C.This work provides a powerful strategy for enabling stable operation of low-temperature zinc-ion capacitors.

An aqueous magnesium-ion hybrid supercapacitor operated at-50℃

The recent advances in aqueous magnesium-ion hybrid supercapacitor(MHSC)have attracted great attention as it brings together the benefits of high energy density,high power density,and synchronously addresses cost and safety issues.However,the freeze of aqueous electrolytes discourages aqueous MHSC from operating at low-temperature conditions.Here,a low-concentration aqueous solution of 4 mol L^(-1) Mg(ClO_(4))_(2) is devised for its low freezing point(-67℃)and ultra-high ionic conductivity(3.37 mS cm^(-1) at-50℃).Both physical characterizations and computational simulations revealed that the Mg(ClO_(4))_(2) can effectively disrupt the original hydrogen bond network among water molecules via transmuting the electrolyte structure,thus yielding a low freezing point.Thus,the Mg(ClO_(4))_(2) electrolytes endue aqueous MHSC with a wider temperature operation range(-50℃–25℃)and a higher energy density of 103.9 Wh kg^(-1) at 3.68 kW kg^(-1) over commonly used magnesium salts(i.e.,MgSO_(4) and Mg(NO_(3))_(2))electrolytes.Furthermore,a quasi-solid-state MHSC based on polyacrylamide-based hydrogel electrolyte holds superior low-temperature performance,excellentflexibility,and high safety.This work pioneers a convenient,cheap,and eco-friendly tactic to procure low-temperature aqueous magnesium-ion energy storage device.

Effect of Anti-freezing Admixtures on Alkali-silica Reaction in Mortars

The influence of anti-freezing admixture on the alkali aggregate reaction in mortar was analyzed with accelerated methods. It is confirmed that the addition of sodium salt ingredients of anti-freezing admixture accelerates the alkali silica reaction to some extent, whereas calcium salt ingredient of anti-freezing admixture reduces the expansion of alkali silica reaction caused by high alkali cement. It is found that the addition of the fly ash considerably suppresses the expansion of alkali silica reaction induced by the anti-freezing admixtures.

Bioinspired anti-freezing 3D-printable conductive hydrogel microfibers for highly-sensitive and wide-range detection of ultralow and high strains

Soft strain sensors that can transduce stretch stimuli into electrical readouts are promising as sustainable wearable electronics.However,most strain sensors cannot achieve highly-sensitive and wide-range detection of ultralow and high strains.Inspired by bamboo structures,anti-freezing microfibers made of conductive poly(vinyl alcohol)hydrogel with poly(3,4-ethylenedioxythiphene)-poly(styrenesulfonate)are developed via continuous microfluidic spinning.The microfibers provide unique bamboo-like structures with enhanced local stress to improve both their length change and resistance change upon stretching for efficient signal conversion.The microfibers allow highlysensitive(detection limit:0.05%strain)and wide-range(0%-400%strain)detection of ultralow and high strains,as well as features of good stretchability(485%strain)and anti-freezing property(freezing temperature:-41.1°C),fast response(200 ms),and good repeatability.The experimental results,together with theoretical foundation analysis and finite element analysis,prove their enhanced length and resistance changes upon stretching for efficient signal conversion.By integrating microfluidic spinning with 3D-printing technique,the textiles of the microfibers can be flexibly constructed.The microfibers and their 3D-printed textiles enable highperformance monitoring of human motions including finger bending and throat vibrating during phonation.This work provides an efficient and general strategy for developing advanced conductive hydrogel microfibers as highperformance wearable strain sensors.

Microscopic Pore Structure of Asphalt Mixture Incorporating with MFL

In order to analyze the microstructure of salt anti-freezing asphalt concrete, i e, MFL（Mafilon） modified asphalt concrete, MIP（mercury intrusion porosity） method was used to obtain the data including porosity and pore size distribution in micro scale. Results show that the porosity grows up with the increase of immersion duration and the salt content. During the immersion, the amount of large pores（60-200 μm） grow up gradually and porosity also grows up correspondingly. Even with different immersion duration, most pores＇ size distribute is beyond 7000 nm.

Rapid self-healing,self-adhesive,anti-freezing,moisturizing,antibacterial and multi-stimuli-responsive PVA/starch/tea polyphenol-based composite conductive organohydrogel as flexible strain sensor

The complexity of application environment stimulates the development of wearable devices based on functional hydrogels.Among all the promising performances,self-healing and self-adhesion properties are ideal for hydrogel sensors,which can guarantee good accuracy,comfort and long service life.However,it is still a challenge to achieve simultaneous self-healing and self-adhesion in different environments(in the air,underwater and at low temperatures).Herein,a feasible new strategy was successfully carried out to prepare a starch-based composite conductive organohydrogel based on the reversible borate ester bonds formed by complexing starch/polyvinyl alcohol(PVA)/tea polyphenol(TP)with borax,and multiple hydrogen-bond interactions among PVA,starch,TP and ethylene glycol(EG).Silver nanoparticles(Ag-NPs),reduced and stabilized by TP,and MWCNTs(multi-walled carbon nanotubes)were introduced into the cross-linking networks to endow the resulting PBSTCE organohydrogel with considerable antibacterial property and conductivity,respectively.The organohydrogel possessed rapid self-healing(HE(self-healing efficiency)=96.07%in 90 s,both in the air and underwater,also at-20℃),considerable self-adhesion(both in the air and underwater,also at-20℃),remarkable stretchability(814%of elongation),anti-freezing(-20℃)and moisture-retention abilities,antibacterial activity,sensitive pH/sugar-responsiveness,and plasticity.The strain sensor formed by the PBSTCE organohydrogel can not only effectively record large-scale human motions(e.g.finger/wrist/elbow bending,walking,etc.),but also accurately capture subtle motion changes(e.g.breathing,chewing,swallowing,speaking,smiling and frowning).Moreover,the self-healed organohydrogel sensor also exhibited almost invariable mechanical,electrical and sensing behaviors.This work demonstrates a feasible strategy to construct multifunctional starch-based organohy-drogels,and promotes their efficient,stable and eco-friendly application as flexible wearable devices.

可穿戴柔性超级电容器用强韧、自修复、抗冻的三角色铁氰化钾氧化还原凝胶聚合物电解质

超级电容器的韧性、自修复和高比电容对于柔性和可穿戴电子设备具有重要的实用价值.为此,我们制备了一种新型的聚乙烯醇-海藻酸钠-铁氰化钾-硫酸钠多功能凝胶聚合物电解质.其中铁氰化钾起到了三角色作用,包括载流子供体、离子交联剂和氧化还原活性剂,有效地缓解了凝胶聚合物电解质通常存在的电导率与机械性能间的矛盾.此外,由于铁氰化钾的氧化还原反应提供了赝电容,组装的超级电容器具有很高的电极比电容和能量密度.该超级电容器还表现出优异的弯曲、拉伸、自修复和抗冻能力.因而,制备的凝胶聚合物电解质和超级电容器在复杂使用条件下的柔性和可穿戴电子设备中具有广阔的应用前景.

Transient Chemical Activation of Covalent Bonds for Healing of Kinetically Stable and Multifunctional Organohydrogels

It remains a great challenge to balance the kinetic stability and intrinsic healing ability of polymer materials.Here,we present an efficient strategy of using a synthetic reaction cycle to regulate the intrinsic healing ability of thermodynamically stable and kinetically inert multifunctional organohydrogels.By combining a double decomposition reaction with spontaneous energy dissipation,we can construct the simplest synthetic reaction cycle that can induce a transient out-of-equilibrium state for achieving the healing of organohydrogels with kinetically locked acylhydrazone bonds.In addition to balancing kinetic stability and healing ability,the synthetic reaction cycle also enables the polymer materials to have high tolerance to organic solvents,high ionic strength,high and low temperatures,and other harsh conditions.Therefore,the kinetically stable and healable organohydrogels remain mechanically flexible and electrically conductive even down to−40°C and are readily recyclable.The integration of chemical networks into healable polymers may provide novel,versatile materials for building next-generation electronic devices.

Cryogenic electrolytes and catalysts for zinc air batteries

The challenges of enabling zinc air batteries to operate at ultralow temperatures are twofold.The Prerequisite is preventing the electrolyte from freezing while maintaining high ionic conductivity.Secondly,the catalyst has to work efficiently at low temperatures.This highlight presents the latest development to resolve the challenges by tuning the structures of the electrolyte and catalyst,offering a new paradigm to widen the working temperature range of zinc air batteries.

Intrinsic electrochemical activity modulation of MOF-derived C/N-NiCoMn-LDH/Ag electrode for low temperature hybrid supercapacitors

Layered double hydroxides(LDHs)are promising electrode candidates for supercapacitors.However,lim-itations like inferior cycling stability and unsatisfactory charge storage capability at low temperatures have exerted negative effects on their applications.Herein,a novel synthetic process has been elaborately designed and provided to have the composition and structure of the C/N-NiCoMn-LDH/Ag(C/N-CNMA)delicately regulated.Both the experimental and theoretical researches unveil that the incorporated manganese species and elemental silver could dramatically modulate the bandgap,crystallinity and surface electron structure of the LDH,leading to the remarkable improvement in its conductivity,exposed active sites and intrinsic electrochemical activity,and thus the OH^(*)and O^(*)adsorption free energy could be remarkably optimized,even at low temperatures.In addition,the low crystallinity C/N-CNMA is of great electrochemical compatibility with both the KOH aqueous electrolyte and the isobutyl alcohol(IPA)modulated organohydrogel electrolyte.By means of adjusting the solvation and hydrogen bonding in the electrolytes,the assembled hybrid supercapacitors deliver excellent energy density,power density and cycling stability in the temperature range of-30 to 25℃.Specifically,the gel electrolyte with IPA as the anti-freezing functional additive displays high flexibility and ionic conductivity at low temperatures.

Concentrated hydrogel electrolyte for integrated supercapacitor with high capacitance at subzero temperature

Hydrogel electrolytes with anti-freezing properties are crucial for flexible quasi-solid-state supercapacitors operating at low temperatures.However,the electrolyte freezing and sluggish ion migration caused by the cold temperature inevitably damage the flexibility and electrochemical properties of supercapacitors.Herein,we introduce the concentrated electrolyte into a freezecasted poly(vinyl alcohol)hydrogel film not only reducing the freezing point of the electrolyte(−51.14℃)in gels for ensuring the flexibility,but also improving the ionic conductivity of the hydrogel electrolyte(5.92 mS cm^(−1)at−40℃)at low temperatures.As a proof,an all-in-one supercapacitor,synthesized by the one-step polymerization method,exhibits a good specific capacitance of 278.6 mF cm^(−2)at−40℃(accounting for 93.8%of the capacitance at room temperature),high rate performance(50%retention under the 100-fold increase in current densities),and long cycle life(88.9%retention after 8,000 cycles at−40℃),representing an excellent low-temperature performance.Our results provide a fresh insight into the hydrogel electrolyte design for flexible energy storage devices operating in the wide range of temperature and open up an exciting direction for improving all-in-one supercapacitors.

具有双离子吸附的多级结构氮掺杂碳球助力超高倍率及稳定的锌离子超级电容器

尽管高能量水系锌离子超级电容器(ZHSCs)的研究取得了重要的进展,但缓慢的锌离子扩散及不理想的阴极材料仍然限制了其能量密度和循环寿命.在本文中,我们设计了具有合适的孔径分布及优异的锌离子储存能力的氮掺杂分级碳球(NMCSs).组装的ZHSCs在0.2 A g^(-1)的电流密度下,表现出优异的电容量(157.8 mA h g^(-1))及能量密度(126.2 W h kg^(-1)),具有卓越的功率密度(39.9 kW kg^(-1)).此外,ZHSCs表现出了超长的循环稳定性,在50,000次循环测试后仍能保持96.2%的初始电容量.此外,我们设计了一种新型的平面ZHSCs,表现出优异的低温电化学性能,超高的体积能量密度(31.6 mW h cm^(-3))和极佳的集成性能.通过原位/非原位表征,系统地揭示了NMCSs电极优异的电化学性能主要来源于阳离子和阴离子的协同吸附以及NMCSs的可逆化学吸附作用机理.本工作不仅为新型高性能ZHSCs的构建和开发提供了新思路,也为进一步理解ZHSCs的电化学储能机理提供了依据.